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Injectable hydrogels with in situ-forming hydrophobic domains: oligo(D,L-lactide) modified poly(olig
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2018-08-31 10:11 581閱讀次數(shù)
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Injectable,insitu-gel領(lǐng)nanostructuredhydrogelshavebeenpreparedfromhydrazideandaldehydefunctionalizedpolymerprecursorsbasedonacopolymerofoligo(ethyleneglycol)methacrylate(OEGMA)andanoligo(lacticacid)macromonomer(OLA)withvaryinglacticacidchainlengths.Theresultinghydrogelscontainamixofchemical(hydrazonebondformationbetweenhydrazideandaldehydegroups)andphysical(hydrophobicinteractionsbetweenOLAchains)cross-linkswhichformcompetitivelyasafunctionoftheOLAchainlengthanddensity.AnincreaseintheOLAchainlengthanddensityresultsintheformationofmorephysicalcross-linksandfewerchemicalcross-links.Tuningtherelativeprevalenceofphysicalandchemicalcross-linkformationfacilitatedlargelyindependenttuningofgelmechanicsrelativetogelswel領(lǐng)anddegradation.Small-angleneutronscatteringoftheseOLA-containinghydrogelsrevealsamicrostructureconsistingofassociativehydrophobicdomains,basedonanincreasedscatteringintensityanddecreasedblobsizerelativetothatobservedforPOEGMAhydrogelspreparedwithouttheOLAco-monomer.ThepresenceofhydrophobicOLAdomainsincreasestheuptakeandslowsthereleaseofbovineserumalbumin,aproteinwell-knowntoassociatewithhydrophobicdomains.Coupledwiththeobservedcytocompatibilityofthereactiveprecursorpolymersusedtopreparethehydrogels,weanticipatesignificantpotentialapplicationsofthesehydrogelsfortheprolongedreleaseofhydrophobiccargoes.
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Injectable hydrogels with in situ-forming hydrophobic domains: oligo(D,L-lactide) modified poly(olig
Injectable,insitu-gel領(lǐng)nanostructuredhydrogelshavebeenpreparedfromhydrazideandaldehydefunctionalizedpolymerprecursorsbasedonacopolymerofoligo(ethyleneglycol)methacrylate(OEGMA)andanoligo(lacticacid)macromonomer(OLA)withvaryinglacticacidchainlengths.Theresultinghydrogelscontainamixofchemical(hydrazonebondformationbetweenhydrazideandaldehydegroups)andphysical(hydrophobicinteractionsbetweenOLAchains)cross-linkswhichformcompetitivelyasafunctionoftheOLAchainlengthanddensity.AnincreaseintheOLAchainlengthanddensityresultsintheformationofmorephysicalcross-linksandfewerchemicalcross-links.Tuningtherelativeprevalenceofphysicalandchemicalcross-linkformationfacilitatedlargelyindependenttuningofgelmechanicsrelativetogelswel領(lǐng)anddegradation.Small-angleneutronscatteringoftheseOLA-containinghydrogelsrevealsamicrostructureconsistingofassociativehydrophobicdomains,basedonanincreasedscatteringintensityanddecreasedblobsizerelativetothatobservedforPOEGMAhydrogelspreparedwithouttheOLAco-monomer.ThepresenceofhydrophobicOLAdomainsincreasestheuptakeandslowsthereleaseofbovineserumalbumin,aproteinwell-knowntoassociatewithhydrophobicdomains.Coupledwiththeobservedcytocompatibilityofthereactiveprecursorpolymersusedtopreparethehydrogels,weanticipatesignificantpotentialapplicationsofthesehydrogelsfortheprolongedreleaseofhydrophobiccargoes.[詳細(xì)]
2018-08-31 10:11
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